{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83056",
      "recalling_firm": "Hitachi America, Ltd., Power Systems Division",
      "address_1": "1840 Old Spanish Trl",
      "address_2": "N/A",
      "postal_code": "77054-2002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts located in AZ, MN, and TN. Foreign distribution to Japan.",
      "recall_number": "Z-1892-2019",
      "product_description": "PROBEAT-V, software versions 4.8.1S, and 5.1M Radiation therapy system.",
      "product_quantity": "3",
      "reason_for_recall": "There is a potential for a discrepant target position when using 3D3D matching mode in PIAS (Positioning Image Analysis System) software installed in the PROBEAT-V, proton therapy systems.",
      "recall_initiation_date": "20190415",
      "center_classification_date": "20190627",
      "termination_date": "20200424",
      "report_date": "20190703",
      "code_info": "2015B01, A01, A02"
    }
  ]
}